A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121161



Internal ID18905100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:22897652..22897930hg38UCSC Ensembl
Outerchr16:22908973..22909251hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1319n106
Supporting Variantsnssv3954438, nssv3966286
SamplesKWS2, KWS1
Known GenesHS3ST2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121161
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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